Canonical Allele Identifier: CA1602344863
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724562A= , CM000667.2:g.174724562A= GRCh38
NC_000005.9:g.174151565A= , CM000667.1:g.174151565A= GRCh37
NC_000005.8:g.174084171A= NCBI36
NG_008124.1:g.4991A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-98A= ENSP00000239243.5:n.-98A=